Medical laboratories - Import export

Medical Device Services / Medical Device Laboratory Testing INVITRO-CONNECT GmbH offers you: - General regulatory advice for medical devices - All regulatory examinations and tests under GLP - Project management and study monitoring - Medical Device Regulatory Service - Product testing for contained SVHC substances INVITRO-CONNECT offers you a complete service for the approval of medical devices according (EU) 2017/745 (Medical Device Regulation - MDR) / ISO 10993. From the development of an ideal test strategy to laboratory and project coordination, study monitoring, toxicological expertise and GLP inspections in the cooperation laboratories. We deliver the finalized test reports including the registration dossier - digitally and on paper, worldwide. Benefit from our diverse know-how, our experienced cooperation partners and an international, very well-organized network. Questions? -> contact@invitro-connect.com

Sensitiv imago® 530 is the previous model in the SensitivE line. Hi-tech hardware-software complexes for diagnostic scan, analysis and healing of organism. Senstiv imago 530 device is being assembled according to the new European quality management standards 9001 full accepted in EU in 2013. The device passed the medical laboratory testing class 2, according to the European Directive.